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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355929생성일: 2026년 10월 25일

2-Methylbenzyl alcohol → (2-Methylphenyl)methyl 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl)benzoate

https://huagongshe.com/reaction/355929

반응식

참여 물질

역할이름HCID투입량
반응물2-Methylbenzyl alcoholHCID 6994—
반응물Sodium hydrideHCID 24758—
반응물4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl]benzoyl chlorideHCID 53802244—
용매TetrahydrofuranHCID 8028—
생성물(2-Methylphenyl)methyl 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)carbonyl)benzoateHCID 8675157532%

반응 단계

To a mixture of 248 mg of 2-methylbenzyl alcohol in 4 ml of anhydrous tetrahydrofuran is added 80 mg of sodium hydride (60% in mineral oil) and the mixture stirred for 1 hour. To the mixture is added 430 mg of 4-[(6,11-dihydro-5H-dibenz[b,e]azepin-5-yl)-carbonyl]benzoyl chloride and the mixture is stirred for 18 hours. The tetrahydrofuran is evaporated in vacuo to a residue which is partitioned between methylene chloride and water. The organic layer is separated and washed with 1N HCl, water, 1M NaHCO3, and brine. The organic layer is dried (Na2SO4) and passed through a short pad of hydrous magnesium silicate and hexane added at the boil to give 170 mg of the desired product, m.p. 140°-142° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834461
출처 데이터셋uspto-grants-1998_11
ORD IDord-03aee920d8d24760bae861837452bc89
출처 메모uspto-grants-1998_11